Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2072671 | 0.752 | 0.280 | 1 | 20589208 | missense variant | A/C | snv | 0.28 | 0.25 | 16 | |
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
rs3811444 | 1 | 247876149 | missense variant | C/T | snv | 0.31 | 0.26 | 12 | |||
rs760077 | 0.925 | 0.120 | 1 | 155208991 | missense variant | T/A | snv | 0.36 | 8 | ||
rs17534202 | 1.000 | 0.120 | 1 | 203312047 | downstream gene variant | G/C | snv | 0.40 | 7 | ||
rs2067079 | 0.807 | 0.240 | 1 | 173866073 | non coding transcript exon variant | C/T | snv | 0.22 | 0.18 | 7 | |
rs1434282 | 1 | 199041592 | non coding transcript exon variant | C/T | snv | 0.76 | 6 | ||||
rs1175550 | 1 | 3774964 | intron variant | A/G | snv | 0.31 | 5 | ||||
rs1569419 | 1 | 3080038 | intron variant | T/C | snv | 0.73 | 5 | ||||
rs2275558 | 0.882 | 0.200 | 1 | 164559883 | missense variant | G/A | snv | 0.30 | 0.19 | 5 | |
rs1052571 | 0.882 | 0.080 | 1 | 15524118 | missense variant | G/A | snv | 0.50 | 0.59 | 4 | |
rs11211480 | 1 | 47227548 | non coding transcript exon variant | A/G | snv | 0.42 | 4 | ||||
rs7529925 | 1 | 199038079 | intron variant | C/T | snv | 0.77 | 4 | ||||
rs12133576 | 1.000 | 0.040 | 1 | 93350843 | intron variant | A/G | snv | 0.51 | 3 | ||
rs2047007 | 1 | 39962303 | intron variant | C/T | snv | 0.17 | 3 | ||||
rs2157691 | 1 | 158613048 | intron variant | G/C | snv | 0.24 | 3 | ||||
rs2246434 | 1 | 158648665 | intron variant | G/A | snv | 0.26 | 0.22 | 3 | |||
rs366684 | 1 | 214013919 | intron variant | G/A;C | snv | 3 | |||||
rs3813803 | 0.925 | 0.080 | 1 | 27955781 | missense variant | T/C | snv | 0.25 | 0.23 | 3 | |
rs533281866 | 1 | 231422308 | intron variant | G/A;C | snv | 3 | |||||
rs857725 | 1 | 158638145 | stop gained | T/A;G | snv | 4.0E-06; 0.28 | 3 | ||||
rs10494964 | 1 | 213793544 | intron variant | T/C | snv | 0.45 | 2 | ||||
rs10910476 | 1 | 234599210 | regulatory region variant | C/A;T | snv | 2 | |||||
rs12734374 | 1.000 | 0.080 | 1 | 155419060 | intron variant | A/T | snv | 3.4E-02 | 2 | ||
rs148046772 | 1 | 156314104 | intron variant | A/C;T | snv | 2 |